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一个偷渡转座子破坏了控制日本牵牛花药用品种花朵和种子颜色的InWDR1基因。

A Stowaway transposon disrupts the InWDR1 gene controlling flower and seed coloration in a medicinal cultivar of the Japanese morning glory.

作者信息

Hoshino Atsushi, Yoneda Yoshiaki, Kuboyama Tsutomu

机构信息

National Institute for Basic Biology.

出版信息

Genes Genet Syst. 2016 Jul 20;91(1):37-40. doi: 10.1266/ggs.15-00062. Epub 2016 Apr 12.

Abstract

Floricultural cultivars of the Japanese morning glory (Ipomoea nil) carry transposons of the Tpn1 family as active spontaneous mutagens. Half of the characterized mutations related to floricultural traits were caused by insertion of Tpn1 family elements. In addition, mutations comprising insertions of several bp, presumed to be footprints generated by transposon excisions, were also found. Among these, ca-1 and ca-2 are 7-bp insertions at the same position in the InWDR1 gene, which encodes a multifunctional transcription regulator. InWDR1 enhances anthocyanin pigmentation in blue flowers and red stems, and promotes dark brown seed pigmentation as well as seed-trichome formation. The recessive ca mutants show white flowers and whitish seeds. We characterized here a white flower and whitish seed line that is used as a medicinal herb. The mutant line carries a novel ca allele named ca-3, which is the InWDR1 gene carrying an insertion of a Stowaway-like transposon, InSto1. The ca-3 allele is the first example of a mutation induced by transposons other than those in the Tpn1 family in I. nil. Because InSto1 and the 7-bp putative footprints are inserted at identical positions in InWDR1, ca-3 is likely to be the ancestor of ca-1 and ca-2. According to Japanese historical records on whitish seeds of I. nil, putative ca mutants appeared at the end of the 17th century, at the latest. This is around one hundred years before the appearance of many floricultural mutants. This suggests that ca-3 is one of the oldest mutations, and that its origin is different from that of most floricultural mutations in I. nil.

摘要

日本牵牛(裂叶牵牛)的花卉栽培品种携带Tpn1家族的转座子,作为活跃的自发诱变剂。与花卉性状相关的已鉴定突变中,有一半是由Tpn1家族元件的插入引起的。此外,还发现了一些由几个碱基对插入组成的突变,推测是转座子切除产生的足迹。其中,ca-1和ca-2是在InWDR1基因同一位置的7个碱基对插入,该基因编码一种多功能转录调节因子。InWDR1增强蓝色花朵和红色茎中的花青素色素沉着,并促进深褐色种子色素沉着以及种子毛状体形成。隐性ca突变体表现为白色花朵和带白色的种子。我们在此对一个用作草药的白色花朵和带白色种子的品系进行了表征。该突变体系携带一个名为ca-3的新ca等位基因,它是InWDR1基因,携带一个类似Stowaway的转座子InSto1的插入。ca-3等位基因是裂叶牵牛中除Tpn1家族转座子以外的转座子诱导突变的首个例子。由于InSto1和7个碱基对的推定足迹插入在InWDR1的相同位置,ca-3可能是ca-1和ca-2的祖先。根据日本关于裂叶牵牛带白色种子的历史记录,推定的ca突变体最晚出现在17世纪末。这比许多花卉突变体出现的时间早大约一百年。这表明ca-3是最古老的突变之一,其起源与裂叶牵牛中大多数花卉突变的起源不同。

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